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Foetal Immune Response Activation and High Replication Rate during Generation of Classical Swine Fever Congenital Infection

Classical swine fever virus (CSFV) induces trans-placental transmission and congenital viral persistence; however, the available information is not updated. Three groups of sows were infected at mid-gestation with either a high, moderate or low virulence CSFV strains. Foetuses from sows infected wit...

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Autores principales: Bohórquez, José Alejandro, Muñoz-González, Sara, Pérez-Simó, Marta, Muñoz, Iván, Rosell, Rosa, Coronado, Liani, Domingo, Mariano, Ganges, Llilianne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7238013/
https://www.ncbi.nlm.nih.gov/pubmed/32295279
http://dx.doi.org/10.3390/pathogens9040285
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author Bohórquez, José Alejandro
Muñoz-González, Sara
Pérez-Simó, Marta
Muñoz, Iván
Rosell, Rosa
Coronado, Liani
Domingo, Mariano
Ganges, Llilianne
author_facet Bohórquez, José Alejandro
Muñoz-González, Sara
Pérez-Simó, Marta
Muñoz, Iván
Rosell, Rosa
Coronado, Liani
Domingo, Mariano
Ganges, Llilianne
author_sort Bohórquez, José Alejandro
collection PubMed
description Classical swine fever virus (CSFV) induces trans-placental transmission and congenital viral persistence; however, the available information is not updated. Three groups of sows were infected at mid-gestation with either a high, moderate or low virulence CSFV strains. Foetuses from sows infected with high or low virulence strain were obtained before delivery and piglets from sows infected with the moderate virulence strain were studied for 32 days after birth. The low virulence strain generated lower CSFV RNA load and the lowest proportion of trans-placental transmission. Severe lesions and mummifications were observed in foetuses infected with the high virulence strain. Sows infected with the moderately virulence strain showed stillbirths and mummifications, one of them delivered live piglets, all CSFV persistently infected. Efficient trans-placental transmission was detected in sows infected with the high and moderate virulence strain. The trans-placental transmission occurred before the onset of antibody response, which started at 14 days after infection in these sows and was influenced by replication efficacy of the infecting strain. Fast and solid immunity after sow vaccination is required for prevention of congenital viral persistence. An increase in the CD8+ T-cell subset and IFN-alpha response was found in viremic foetuses, or in those that showed higher viral replication in tissue, showing the CSFV recognition capacity by the foetal immune system after trans-placental infection.
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spelling pubmed-72380132020-05-28 Foetal Immune Response Activation and High Replication Rate during Generation of Classical Swine Fever Congenital Infection Bohórquez, José Alejandro Muñoz-González, Sara Pérez-Simó, Marta Muñoz, Iván Rosell, Rosa Coronado, Liani Domingo, Mariano Ganges, Llilianne Pathogens Article Classical swine fever virus (CSFV) induces trans-placental transmission and congenital viral persistence; however, the available information is not updated. Three groups of sows were infected at mid-gestation with either a high, moderate or low virulence CSFV strains. Foetuses from sows infected with high or low virulence strain were obtained before delivery and piglets from sows infected with the moderate virulence strain were studied for 32 days after birth. The low virulence strain generated lower CSFV RNA load and the lowest proportion of trans-placental transmission. Severe lesions and mummifications were observed in foetuses infected with the high virulence strain. Sows infected with the moderately virulence strain showed stillbirths and mummifications, one of them delivered live piglets, all CSFV persistently infected. Efficient trans-placental transmission was detected in sows infected with the high and moderate virulence strain. The trans-placental transmission occurred before the onset of antibody response, which started at 14 days after infection in these sows and was influenced by replication efficacy of the infecting strain. Fast and solid immunity after sow vaccination is required for prevention of congenital viral persistence. An increase in the CD8+ T-cell subset and IFN-alpha response was found in viremic foetuses, or in those that showed higher viral replication in tissue, showing the CSFV recognition capacity by the foetal immune system after trans-placental infection. MDPI 2020-04-14 /pmc/articles/PMC7238013/ /pubmed/32295279 http://dx.doi.org/10.3390/pathogens9040285 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Bohórquez, José Alejandro
Muñoz-González, Sara
Pérez-Simó, Marta
Muñoz, Iván
Rosell, Rosa
Coronado, Liani
Domingo, Mariano
Ganges, Llilianne
Foetal Immune Response Activation and High Replication Rate during Generation of Classical Swine Fever Congenital Infection
title Foetal Immune Response Activation and High Replication Rate during Generation of Classical Swine Fever Congenital Infection
title_full Foetal Immune Response Activation and High Replication Rate during Generation of Classical Swine Fever Congenital Infection
title_fullStr Foetal Immune Response Activation and High Replication Rate during Generation of Classical Swine Fever Congenital Infection
title_full_unstemmed Foetal Immune Response Activation and High Replication Rate during Generation of Classical Swine Fever Congenital Infection
title_short Foetal Immune Response Activation and High Replication Rate during Generation of Classical Swine Fever Congenital Infection
title_sort foetal immune response activation and high replication rate during generation of classical swine fever congenital infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7238013/
https://www.ncbi.nlm.nih.gov/pubmed/32295279
http://dx.doi.org/10.3390/pathogens9040285
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